jund[All Fields] AND 1[has_clinical] - dbVar - NCBI

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Items: 19

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Number of Variants: 19

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv3909384	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 18,389,135-18,392,751 , GRCh38.p12 chr19: 18,278,325-18,281,941	JUND, MIR3188
nsv3899187	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 18,391,070-18,393,112 , GRCh38.p12 chr19: 18,280,260-18,282,302	JUND, MIR3188
nsv3901891	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 18,391,070-18,392,873 , GRCh38.p12 chr19: 18,280,260-18,282,063	JUND, MIR3188
nsv3908879	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 18,391,070-18,392,751 , GRCh38.p12 chr19: 18,280,260-18,281,941	JUND, MIR3188
nsv3899752	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 18,392,236-18,392,751 , GRCh38.p12 chr19: 18,281,426-18,281,941	JUND, MIR3188
nsv3915387	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 18,033,043-18,573,963 , NCBI36 chr19: 17,894,043-18,434,963 , GRCh38 chr19: 17,922,234-18,463,153	JUND, CSP3, 28 more genes
nsv3904885	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 68,029-59,110,290 , GRCh38.p12 chr19: 68,029-58,598,923	JUND, ZNF321P, 2443 more genes
nsv3903203	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-59,097,160 , GRCh38.p12 chr19: 260,912-58,585,793	JUND, BABAM1, 2426 more genes
nsv3903092	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr19: 260,912-58,956,888 , GRCh38.p12 chr19: 260,912-58,445,521	JUND, LENG8, 2408 more genes
nsv3913730	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 11,199,618-49,821,491 , GRCh37 chr19: 11,338,618-45,129,651 , GRCh38 chr19: 11,227,942-44,626,354	JUND, BCKDHA, 1102 more genes
nsv3914228	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr19: 17,148,576-40,106,894 , GRCh38 chr19: 17,176,767-34,924,150 , GRCh37 chr19: 17,287,576-35,415,054	JUND, LOC105372355, 411 more genes
nsv3922457	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,085,489-28,330,584 , GRCh38 chr19: 13,974,677-27,839,676 , NCBI36 chr19: 13,946,489-33,022,424	JUND, REX1BD, 416 more genes
nsv3921076	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr19: 15,133,594-24,193,591 , GRCh37 chr19: 15,244,405-24,376,393 , NCBI36 chr19: 15,105,405-24,168,233	JUND, MRPL34, 358 more genes
nsv3895942	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 16,526,787-24,631,604 , GRCh38.p12 chr19: 16,415,976-24,448,802	JUND, BNIP3P37, 307 more genes
nsv4729750	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr19: 14,286,624-20,956,753 , GRCh38.p12 chr19: 14,175,812-20,773,947	JUND, LOC105372309, 269 more genes
nsv3899892	copy number variation	1	nstd102	human	Benign	GRCh37 chr19: 18,332,984-18,540,644 , GRCh38.p12 chr19: 18,222,174-18,429,834	JUND, LSM4, 12 more genes
nsv3923519	copy number variation	1	nstd102	human	Uncertain significance	GRCh38 chr19: 18,133,970-18,424,117 , GRCh37 chr19: 18,244,780-18,534,927 , NCBI36 chr19: 18,105,780-18,395,927	JUND, RPL39P38, 18 more genes
nsv7095477	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 17,927,663-19,312,528 , GRCh38.p12 chr19: 17,816,854-19,201,719	JUND, BORCS8, 60 more genes
nsv6314002	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr19: 18,327,675-18,543,341 , GRCh38.p12 chr19: 18,216,865-18,432,531	JUND, MIR3188, 13 more genes

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